A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564117



Internal ID18862398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:14071214..14285512hg38UCSC Ensembl
Innerchr18:14071213..14285511hg19UCSC Ensembl
Innerchr18:14061213..14275511hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38214299
hg19214299
hg18214299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060497
Supporting Variants
Samples
Known GenesANKRD20A5P, ZNF519
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564117
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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